Product NDC: | 57520-0303 |
Proprietary Name: | Renaforce |
Non Proprietary Name: | Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum, |
Active Ingredient(s): | 3; 3; 12; 12; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum, |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57520-0303 |
Labeler Name: | Apotheca Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20101102 |
Package NDC: | 57520-0303-1 |
Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0303-1) |
NDC Code | 57520-0303-1 |
Proprietary Name | Renaforce |
Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0303-1) |
Product NDC | 57520-0303 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum, |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20101102 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Apotheca Company |
Substance Name | BERBERIS VULGARIS ROOT BARK; ECHINACEA ANGUSTIFOLIA; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; POTASSIUM CHLORIDE; PROTORTONIA CACTI |
Strength Number | 3; 3; 12; 12; 12; 12 |
Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |